Search Results - "Qin, Danqing"

Abnormal hemoglobin anti-Lepore Hong Kong compound with β0-thalassemia ameliorate thalassemia severity when co-inherited with α-thalassemia by Bao, Xiuqin, Wang, Jicheng, Qin, Danqing, Yao, Cuize, Liang, Jie, Liang, Kailing, Du, Li

“…Abnormal hemoglobin anti-Lepore Hong Kong is a rare βδ fusion variants resulting from non-homologous crossover during meiosis. Anti-Lepore Hong Kong is known…”
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Comparison of cord blood hematological parameters among normal, α-thalassemia, and β-thalassemia fetuses between 17 and 38 weeks of gestation by Zhan, Wenli, Guo, Hao, Hu, Siqi, Wang, Jicheng, Qin, Danqing, Liang, Juqing, Du, Li, Luo, Mingyong

“…The aim of this study was to retrospectively compare hematological parameters among normal, α-, and β-thalassemia fetuses between 17 and 38 weeks of gestation…”
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Hb Q-Thailand heterozygosity unlinked with the (-α4.2/) α+-thalassemia deletion allele identified by long-read SMRT sequencing: hematological and molecular analyses by Qin, Danqing, Wang, Jicheng, Yao, Cuize, Bao, Xiuqin, Liang, Jie, Du, Li

“…In the present study, two unrelated cases of Hb Q-Thailand heterozygosity unlinked with the (-α 4.2 /) α + -thalassemia deletion allele were identified by…”
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Serum lipidome reveals lipid metabolic dysregulation in severe fever with thrombocytopenia syndrome by Guo, Shuai, Yan, Yunjun, Zhang, Jingyao, Yang, Zhangong, Tu, Lirui, Wang, Chunjuan, Kong, Ziqing, Wang, Shuhua, Wang, Baojie, Qin, Danqing, Zhou, Jie, Wang, Wenjin, Hao, Yumei, Guo, Shougang

“…Severe fever with thrombocytopenia syndrome (SFTS) is a rapidly progressing infectious disease with a high fatality rate caused by a novel bunyavirus (SFTSV)…”
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The prevalence and molecular spectrum of α- and β-globin gene mutations in 14,332 families of Guangdong Province, China by Yin, Aihua, Li, Bing, Luo, Mingyong, Xu, Longchang, Wu, Li, Zhang, Liang, Ma, Yuanzhu, Chen, Tingting, Gao, Shuang, Liang, Juqing, Guo, Hao, Qin, Danqing, Wang, Jicheng, Yuan, Tenglong, Wang, Yixia, Huang, Wei-wei, He, Wen-Fei, Zhang, Yanxia, Liu, Chang, Xia, Sujian, Chen, Qingshan, Zhao, Qingguo, Zhang, Xiaozhuang

“…To reveal the familial prevalence and molecular variation of α- and β-globin gene mutations in Guangdong Province. A total of 40,808 blood samples from 14,332…”
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Compound heterozygosity for hemoglobin variant Hb-Broomhill and the Southeast Asian α-thalassemia deletion does not worsen outcome: a case report of two unrelated patients by Qin, Danqing, Du, Li, Wang, Jicheng, Yao, Cuize, Guo, Hao, Yuan, Tenglong, Liang, Jie, Yin, Aihua

“…We report two unrelated cases of compound heterozygosity for hemoglobin (Hb) variant Broomhill and the Southeast Asian (- - SEA/) α-thalassemia deletion, whose…”
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Magnetic resonance imaging-guided disc–condyle relationship adjustment via articulation: a technical note and case series by Xiong, Xin, Yin, Xiaoli, Liu, Fang, Qin, Danqing, Liu, Yang

“…A normal disc–condyle relationship is crucial to the health and function of the temporomandibular joint. We herein introduce a novel technique that can…”
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First study to describe a novel HbA2: c.400A > C mutation and Hb Dongguan heterozygote in two unrelated Chinese families by Yao, Cuize, Qin, Danqing, Wang, Jicheng, Bao, Xiuqin, Liang, Jie, Du, Li

“…Here we report two rare α-globin chain variants in two unrelated families: Hb Val de Marne [α133(H16) Ser > Arg (AGC > CGC); HBA2: c.400A > C] and Hb Dongguan…”
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Severe fetal anemia and hydrops fetalis associated with compound heterozygosity for Hb Zurich-Albisrieden (HBA2:c.178G>C) and Hb Quong Sze (HBA2:c.377T>C) by Du, Li, Bao, Xiuqin, He, Wei, Qin, Danqing, Wang, Jicheng, Xiong, Ying, Shi, Xiaomei, Ding, Hongke, Yao, Cuize, Wu, Jing

“…We report on a fetus with cardiomegaly and increased middle cerebral artery-peak systolic velocity at 25 weeks of gestation. Severe fetal anemia (hemoglobin…”
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Accurate detection of α-globin gene copy number variants with two reactions using droplet digital PCR by Bao, Xiuqin, Qin, Danqing, Ma, Jian, Zhou, Xiangcheng, Wang, Jicheng, Yao, Cuize, Zhang, Liang, Du, Li

“…The α-thalassemia is a highly prevalent disease in tropical and subtropical regions, including southern China, and is mainly caused by deletion in α-globin…”
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Identification of four novel large deletions and complex variants in the α-globin locus in Chinese population by Bao, Xiuqin, Wang, Jicheng, Qin, Danqing, Yao, Cuize, Liang, Jie, Liang, Kailing, Zeng, Yukun, Du, Li

“…At present, the methods generally used to detect α-thalassemia mutations are confined to detecting common mutations, which may lead to misdiagnosis or missed…”
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The first Chinese case of unstable Hemoglobin Santa Ana detected by capillary electrophoresis: a case report and literature review by Du, Li, Qin, Danqing, Wang, Jicheng, Yao, Cuize, Zhu, Juan, Guo, Hao, Yuan, Tenglong, Liang, Jie, Yin, Aihua

“…Hemoglobin Santa Ana [β88(F4)Leu→Pro (CTG > CCG) : c.266T > C] is an unstable hemoglobin variant characterized by a substitution of the amino acid leucine by…”
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Two novel deletion mutations in β-globin gene cause β-thalassemia trait in two Chinese families by Bao, Xiuqin, Qin, Danqing, Wang, Jicheng, Chen, Jing, Yao, Cuize, Liang, Jie, Liang, Kailing, Wang, Yixia, Wang, Yousheng, Du, Li, Yin, Aihua

“…β-Thalassemia is mainly caused by point mutations in the β-globin gene cluster. With the rapid development of sequencing technic, more and more variants are…”
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Characterisation of two unusual cases of haemoglobin Bart’s hydrops foetalis caused by –SEA and large novel α-globin gene cluster deletions by Wang, Yunan, Xiong, Ying, Liu, Chang, Lu, Jian, Wang, Jicheng, Qin, DanQing, Liu, Ling, Wu, Jing, Zhao, Xin, Fang, Liyuan, Du, Li, Yin, Aihua

“…Background We describe 2 unusual haemoglobin (Hb) Bart’s hydrops cases that could not be explained by traditional factors. Case presentation: Two families with…”
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Characterisation of two unusual cases of haemoglobin Bart’s hydrops foetalis caused by – and large novel α-globin gene cluster deletions by Yunan Wang, Ying Xiong, Chang Liu, Jian Lu, Jicheng Wang, DanQing Qin, Ling Liu, Jing Wu, Xin Zhao, Liyuan Fang, Li Du, Aihua Yin

“…Background We describe 2 unusual haemoglobin (Hb) Bart’s hydrops cases that could not be explained by traditional factors. Case presentation: Two families with…”
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The -α3.7III subtype of α+-thalassemia was identified in China by Bao, Xiuqin, Wang, Jicheng, Qin, Danqing, Zhang, Rui, Yao, Cuize, Liang, Jie, Liang, Kailing, Du, Li

“…The 3.7 kb deletion (-α 3.7 ) in the α-globin cluster, which characterizes α + -thalassemia, has been reported to have a carrier rate of 4.78% in southern…”
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Compounded with hemoglobin Port Phillip and ‐α4.2 or ‐‐SEA deletions were identified in Chinese population by Du, Li, Bao, Xiuqin, Qin, Danqing, Wang, Jicheng, Yao, Cuize, Liang, Jie, Chen, Jianhong, Yin, Aihua

“…Introduction Although over 1000 hemoglobin (Hb) variants were identified so far, Hb Port Phillip compound with α‐thalassemia deletion had no reported before…”
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Ferroptosis and central nervous system demyelinating diseases by Qin, Danqing, Li, Dong, Wang, Chunjuan, Guo, Shougang

“…Ferroptosis is a newly discovered programmed cell death caused by intracellular iron excess and glutathione (GSH) system imbalance, resulting in fatal lipid…”
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Exosomal miR-23a-3p derived from human umbilical cord mesenchymal stem cells promotes remyelination in central nervous system demyelinating diseases by targeting Tbr1/Wnt pathway by Qin, Danqing, Wang, Chunjuan, Li, Dong, Guo, Shougang

“…Oligodendrocyte precursor cells are present in the adult central nervous system, and their impaired ability to differentiate into myelinating oligodendrocytes…”
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Soft tissue chondrosarcoma occurred in the left parotid region: a case report by Ting, Shen, Lina, Zhang, Ning, Geng, Yaling, Tang, Danqing, Qin, Dongping, Ren, Yu, Chen

“…Chondrosarcoma is extremely rare in maxillofacial soft tissue. A case diagnosed as well-differentiated chon- drosarcoma in the left parotid region was…”
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